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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

556 related items for PubMed ID: 17654068

  • 21.
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  • 22. Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].
    Phylipsen M, Prior JF, Lim E, Lingam N, Finlayson J, Arkesteijn SG, Harteveld CL, Giordano PC.
    Hemoglobin; 2010 Jan; 34(2):123-6. PubMed ID: 20353346
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  • 24. Two independent origins of Hb Dhonburi (Neapolis) [beta 126 (H4) Val-->Gly]: an electrophoretically silent hemoglobin variant.
    Viprakasit V, Chinchang W.
    Clin Chim Acta; 2007 Feb; 376(1-2):179-83. PubMed ID: 17007829
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  • 27. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
    Changtrakun Y, Fucharoen S, Ayukarn K, Siriratmanawong N, Fucharoen G, Sanchaisuriya K.
    Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
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  • 30. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S, Ayukarn K, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
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  • 31. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL, Steen G, Vlasveld LT, van Delft P, Giordano PC.
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
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  • 32. Spontaneous mutation of the hemoglobin Leiden (beta 6 or 7 Glu-->0) in a Thai girl.
    Sanguansermsri P, Shimbhu D, Wongvilairat R, Pimsorn C, Sanguansermsri T.
    Haematologica; 2003 Dec; 88(12):ECR35. PubMed ID: 14688008
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  • 33. Characterization of Hb Calvino (HBB: c.406G > A): a new silent β-globin gene variant found in coexistence with α-thalassemia in a family of African origin.
    Marsella M, Salvagno G, Dolcini B, Ferlini A, Ravani A, Harteveld CL, Giordano PC, Borgna-Pignatti C.
    Hemoglobin; 2014 Dec; 38(5):369-72. PubMed ID: 25222042
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  • 36. alpha-Thalassaemia due to a single codon deletion in the alpha1-globin gene. Computational structural analysis of the new alpha-chain variant. Mutations in brief no. 132. Online.
    Ayala S, Colomer D, Gelpí JL, Corrons JL.
    Hum Mutat; 1998 Dec; 11(5):412. PubMed ID: 10206681
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  • 39. Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method.
    Sura T, Trachoo O, Viprakasit V, Vathesatogkit P, Tunteeratum A, Busabaratana M, Wisedpanichkij R, Isarangkura P.
    Ann Hematol; 2007 Sep; 86(9):659-63. PubMed ID: 17503046
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  • 40. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
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